| Literature DB >> 33657948 |
Dan Wang1, Yimeng Du1, Wenpeng Zhang1, Xiaolu Han1, Hui Zhang1, Zengming Wang1, Nan Liu1, Meng Li1, Xiang Gao1, Xiaomei Zhuang1, Jing Gao1, Aiping Zheng1.
Abstract
For efficient intranasal transport of parathyroid hormone (1-34) [PTH(1-34)], there is a great medical need to investigate permeation enhancers for intranasal formulations. In this study, the development of PTH(1-34) intranasal formulations was conducted. Based on conformation and chemical stability studies, the most preferable aqueous environment was determined to be 0.008 M acetate buffer solution (ABS). Subsequently, citric acid and Kolliphor® HS·15 were compared as permeation enhancers. The mechanisms of action of citric acid and Kolliphor® HS·15 were investigated using an in vitro model of nasal mucosa, and Kolliphor® HS·15 led to higher permeability of fluorescein isothiocyanate-labeled PTH(1-34) (FITC-PTH) by enhancing both the transcellular and paracellular routes. Moreover, citric acid showed severe mucosal toxicity resulting in cilia shedding, while Kolliphor® HS·15 did not cause obvious mucosa damage. Finally, Kolliphor® HS·15 was studied as a permeation enhancer using a liquid chromatography tandem mass spectrometry (LC-MS/MS) method. The results showed that 5% and 10% Kolliphor® HS·15 increased the bioavailability of PTH(1-34) to 14.76% and 30.87%, respectively. In conclusion, an effective and biosafe PTH(1-34) intranasal formulation was developed by using 10% Kolliphor® HS·15 as a permeation enhancer. Intranasal formulations with higher concentrations of Kolliphor® HS·15 for higher bioavailability of PTH(1-34) could be further researched.Entities:
Keywords: Parathyroid hormone (1-34); intranasal formulation; mucosal toxicity; permeation enhancer; pharmacokinetics
Year: 2021 PMID: 33657948 PMCID: PMC7935113 DOI: 10.1080/10717544.2021.1889718
Source DB: PubMed Journal: Drug Deliv ISSN: 1071-7544 Impact factor: 6.419